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Role of CDC42 in pro-inflammatory phenotype of senescent vascular endothelial cells

Research Project

Project/Area Number 24790272
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field General medical chemistry
Research InstitutionChiba University

Principal Investigator

ITO Takashi  千葉大学, 医学部附属病院, 特任助教 (20597124)

Research Collaborator MINAMINO Tohru  新潟大学, 医歯学総合研究科, 教授 (90328063)
Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2013: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2012: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords慢性炎症 / 細胞老化 / 血管内皮細胞 / CDC42 / 動脈硬化 / 寿命 / 老化 / PAK2 / 個体老化
Research Abstract

Chronic inflammation underlies most age-related diseases such as cancer, cardiovascular disease, and neurodegenerative disorder. This research focuses on a phenomenon called cellular senescence, in which multiple genes associated with inflammation are upregulated. We identified CDC42 as a regulator of inflammatory genes in senescent vascular cells, and also as a regulator of atherosclerosis in mice. CDC42 was the cause of short lifespan of mutant worms with immune over activation, a model for chronic inflammation of mammals. These results suggest that CDC42 has a critical role in chronic inflammation and age-related diseases.

Report

(3 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • Research Products

    (6 results)

All 2013 2012 Other

All Presentation (6 results) (of which Invited: 2 results)

  • [Presentation] CDC42経路が老化血管内皮細胞の炎症誘導を制御する2013

    • Author(s)
      伊藤孝, 南野徹
    • Organizer
      第13回日本抗加齢医学総会
    • Related Report
      2013 Final Research Report
    • Invited
  • [Presentation] 老化血管内皮細胞による炎症誘導にCDC42経路とNFκB経路が寄与する2012

    • Author(s)
      伊藤孝, 南野徹
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      (ポスター発表かつ口頭発表)
    • Related Report
      2013 Final Research Report
  • [Presentation] CDC42 and NFκB signaling contribute to pro-inflammatory phenotype of senescent endothelial cells2012

    • Author(s)
      Ito T, Minamino T
    • Organizer
      Keystone Symposium Aging and Diseases of Aging(S2)
    • Place of Presentation
      (ポスター発表かつ口頭発表, Travel award受賞)
    • Related Report
      2013 Final Research Report
  • [Presentation] CDC42 and NFκB signaling contribute to pro-inflammatory phenotype of senescent endothelial cells2012

    • Author(s)
      Ito T, Minamino T
    • Organizer
      41st Annual Meeting of The American Aging Association
    • Place of Presentation
      (口頭発表)
    • Related Report
      2013 Final Research Report
  • [Presentation] CDC42 and NFκB signaling contribute to pro-inflammatory phenotype of senescent endothelial cells.2012

    • Author(s)
      伊藤 孝
    • Organizer
      Keystone Symposium on Aging and Diseases of Aging (S2)
    • Place of Presentation
      東京
    • Related Report
      2012 Research-status Report
  • [Presentation] CDC42経路が老化血管内皮細胞の炎症誘導を制御する

    • Author(s)
      伊藤 孝
    • Organizer
      第13回日本抗加齢医学総会
    • Place of Presentation
      横浜パシフィコ
    • Related Report
      2013 Annual Research Report
    • Invited

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Published: 2013-05-31   Modified: 2019-07-29  

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